Benzimidazoles, processes for their preparation and pharmaceutical preparations containing such compounds

ABSTRACT

The invention relates to 2-carboethoxyamino-5(6)-(2-amino-5-thiazoloyl)-benzimidazole compounds with anthelmintic properties and to processes for their preparation and pharmaceutical preparations containing such compounds.

This is a continuation of application Ser. No. 061,097 filed on July 26,1979, U.S. Pat. No. 4,297,365.

The invention relates to novel benzimidazoles, especiallybenzimidazolecarbamates of the formula I ##STR1## in which R₁ is asubstituted or unsubstituted hydrocarbon radical of aliphatic,cycloaliphatic, cycloaliphaticaliphatic or aromatic character, R₂ ishydrogen or a substituted or unsubstituted hydrocarbon radical ofaliphatic character and R₃ and R₄ are hydrogen or a substituted orunsubstituted hydrocarbon radical of aliphatic, cycloaliphatic oraromatic character, or taken together are a substituted or unsubstituteddivalent hydrocarbon radical of aliphatic character, in which the carbonatoms of the chain can be interrupted by a hetero-atom, their tautomericcompounds and salts and processes for their preparation, the compoundsof the formula I and their salts as pharmacologically active compounds,pharmaceutical preparations containing such compounds and the use of thenovel compounds as pharmacologically active substances and for theproduction of pharmaceutical preparations.

In this specification the term "lower" used to qualify radicals andcompounds denotes that these contain preferably not more than 7 and inparticular not more than 4 carbon atoms.

An aliphatic hydrocarbon radical R₁, R₂ or R₃, which can be substituted,is in particular an alkyl radical or an alkenyl or alkynyl radical,especially a straight-chain or branched lower alkyl radical or loweralkenyl or lower alkynyl radical. Substituents of aliphatic hydrocarbonradicals are, for example, free, esterified or etherified hydroxylgroups, such as lower alkanoyloxy, lower alkoxy or lower alkenyloxygroups, or halogen atoms, and also free or esterified carboxyl groups,such as lower alkoxycarbonyl.

Lower alkyl groups are, for example, preferably methyl groups and alsoethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec.-butyl, tert.-butyl,n-pentyl, isopentyl, neopentyl, n-hexyl, isohexyl or n-heptyl groups;lower alkenyl groups are, for example, the allyl group or the2-methylallyl group, and lower alkynyl groups are preferably propargylgroups. Substituted lower alkyl groups are, for example, thetrifluoromethyl group or a free or esterified carboxymethyl group, forexample a lower alkoxycarbonylmethyl group, for example amethoxycarbonylmethyl group.

Lower alkoxy is, for example, methoxy, ethoxy, n-propoxy, isopropoxy,n-butoxy or n-pentyloxy and lower alkenyloxy is, for example, vinyloxyor allyloxy.

Halogen atoms are in particular fluorine, chlorine or bromine atoms, butcan also be iodine atoms.

A cycloaliphatic hydrocarbons radical is in particular a monocyclic orpolycyclic cycloalkyl radical having, for example, not more than 12 andpreferably 3 to 10 ring carbon atoms.

A cycloalkyl group is, for example, a cyclopropyl, cyclobutyl,cyclopentyl, cyclohexyl, cycloheptyl or adamantyl group.

In a cycloaliphatic-aliphatic hydrocarbon radical R₁, the cycloaliphaticradical is, for example, as defined above and is preferably a cycloalkylradical. The aliphatic moiety of such a cycloaliphatic-aliphatic radicalis, for example, an alkylene radical, preferably a lower alkyleneradical.

A cycloalkyl-lower alkyl group is, for example, a cyclopropylmethyl,cyclopropyl-1,1- or -1,2-ethyl, cyclopentylmethyl, cyclopentyl-1,1- or-1,2-ethyl or cyclopentyl-1,2- or -1,3-propyl, cyclohexylmethyl,cyclohexyl-1,1- or -1,2-ethyl or cyclohexyl-1,2- or -1,3-propyl orcycloheptylmethyl radical.

As hydrocarbon radicals of aromatic character, the substituents R₁, R₃and R₄ can be a carbocyclic aromatic radical or a heterocyclic radicalof aromatic character. A carbocyclic aromatic radical is a monocyclic orbicyclic radical, for example naphthyl, but especially phenyl, which canbe substituted by one, two or more identical or different substituents.Such substituents are, for example, hydrocarbon radicals, such as loweraliphatic hydrocarbons radicals, for example lower alkyl, free orfunctionally modified hydroxyl or mercapto, such as etherified hydroxyl,for example lower alkoxy, lower alkenyloxy or lower alkylenedioxy, andalso lower alkylthio, or halogen, trifluoromethyl, nitro, amino,including substituted amino, for example lower alkylamino or di-loweralkylamino, and free or functionally modified carboxyl, such asesterified carboxyl, for example lower alkoxycarbonyl.

A heterocyclic radical of aromatic character is in particular amonocyclic or also a bicylic, monoazacyclic, monooxacyclic ormonothiacyclic radical of aromatic character, which, for example, can besubstituted in the same way as the aromatic hydrocarbon radicalmentioned above. The heterocyclic radical can be bonded in any positionand is, for example, pyrrolyl, pyridyl, quinolyl, furyl or thienyl.

Pyrrolyl is, for example, pyrrol-2-yl or pyrrol-3-yl, pyridyl is, forexample, 2-, 3- or 4-pyridyl, quinolyl is, for example, 2-, 3- or4-quinolyl, furyl is, for example, 2- or 3-furyl and thienyl is, forexample, 2- or 3-thienyl.

Substituents on the nitrogen atom are, for example, lower alkylradicals, for example methyl, ethyl, n-propyl, isopropyl, n-butyl,n-pentyl or n-hexyl, or aromatic hydrocarbon radicals, for example asubstituted or unsubstituted phenyl radical, as already described above.

The two substituents R₃ and R₄ taken together can also be a substitutedor unsubstituted divalent aliphatic hydrocarbon radical having 4-7carbon atoms in the chain.

The group -NR₃ R₄ in the 2-position of the thiazole ring is, forexample, lower alkylamino or di-lower alkylamino, for examplemethylamino, dimethylamino, ethylamino, diethylamino, n-propylamino,di-n-propylamino, isopropylamino, di-isopropylamino or di-n-butylamino.This group is, however, also lower alkyleneamino, in which the loweralkylene chain can be interrupted, for example by a hetero-atom, forexample oxygen, sulfur or substituted or unsubstituted nitrogen, and is,for example, lower alkyleneamino, for example, pyrrolidino,2,5-dimethylpyrrolidino, piperidino, 2-methylpiperidino,hexahydroazepino or octahydroazocino, oxa-lower alkyleneamino, forexample morpholino, thia-lower alkyleneamino, for examplethiomorpholino, and aza-lower alkyleneamino, for example piperazino orN-methyl- or N-phenyl-piperazino.

The novel compounds have valuable pharmacological properties. They makepossible an advance in the control of parasitic helminths, i.e. in thetreatment of parasitic infections by helminths. The term "helminths"relates to nematodes, cestodes and trematodes, ie. to worms which in themain infest the gastrointestinal tract, the liver and also other organs.The compounds are in the main particularly suitable for controllingparasitic nematodes, for example Ascaridae, Trichostrongylidae,Strongylidae and Ancylostomatidae (hookworm), and cestodes, for exampleTaeniidae and Anoplocephalidae, and trematodes, for example Fasciolodae.

When administered orally in doses of 10 to 100 mg/kg or parenterally indoses of 5 to 25 mg/kg to animals, for example to hamsters which havebeen experimentally infested with Necator americanus or Ancylostomaceylanicum or to dogs which have become naturally infected withAncylostoma caninum, the novel compounds eliminate the correspondingworms.

The novel compounds mentioned are suitable as agents having ananthelmintic action, especially as agents against hookworm.

The invention relates in particular to compounds of the formula I inwhich R₁ is lower alkyl, cycloalkyl or phenyl, R₂ is hydrogen or loweralkyl and R₃ and R₄ are each hydrogen, lower alkyl, lower alkenyl,cycloalkyl or phenyl, which is unsubstituted or substituted, for exampleby lower alkyl, lower alkoxy or halogen, or R₃ and R₄ taken together area lower alkylene chain, which can be interrupted by an oxygen or sulfuratom or by a nitrogen atom which can be substituted, for example bylower alkyl, and their tautomeric compounds and salts.

The invention relates especially to those compounds of the formula I inwhich R₁ is lower alkyl, R₂ is hydrogen or lower alkyl and R₃ and R₄ areeach hydrogen, lower alkyl, lower alkenyl, cycloalkyl or phenyl, or R₃and R₄ taken together with the adjacent nitrogen atom are loweralkyleneamino, for example pyrrolidino or piperidino, and theirtautomeric compounds and salts, especially the pharmaceutically usablenon-toxic salts.

Compounds of the formula I which are of particular interest in thisinvention are those in which R₁ is lower alkyl, for example methyl orethyl, R₂ is lower alkyl, for example methyl or ethyl, R₃ is hydrogenand R₄ is lower alkyl, for example methyl, ethyl, n-propyl, isopropyl,n-butyl or isobutyl, and their tautomeric compounds and salts,especially pharmaceutically usable, non-toxic salts.

The compounds of the formula I described in the examples, and theirsalts, especially their pharmaceutically usable, non-toxic salts, areparticularly preferred.

The novel benzimidazoles of the formula I are obtained by methods knownper se.

Thus, for example, the novel benzimidazoles of the formula I can beobtained by reacting a substituted o-phenylenediamine derivative of theformula II ##STR2## in which R₂, R₃ and R₄ are as defined under formulaI, or a salt thereof, with a compound of the formula III ##STR3## inwhich R_(x) is hydrogen or the COOR₁ group and R_(y) is the cyano group,or R_(x) and R_(y) taken together are a disubstituted methylene group ofthe formula ##STR4## in which R_(z) ¹ is an alkylthio or arylthio groupand R_(z) ² is an alkylthio or arylthio group, an amino group or theNHCOOR₁ group, and, if desired, carrying out additional process steps.

The compounds of the formula III which are used in the process describedare, for example, compounds of the type having the formulae NC-NH-COOR₁,NC-N(COOR₁)₂, ##STR5##

Compounds of the formula III are obtained by acylating the correspondingcyanamides or isothiourea compounds with compounds which donate thegroup COOR₁. For example, monoacylated S-lower alkyl-isothioureas ordiacylated S-lower alkyl-isothioureas in which the acyl radical is aCOOR₁ group can be obtained by reacting S-lower alkyl-isothioureas withone or two equivalents of a suitable halogenoformate Hal-COOR₁ in acooled aqueous or alcoholic medium, if necessary in the presence of abase. If desired, the corresponding reaction mixture can also beobtained in situ in that reaction medium in which the subsequentreaction with the corresponding thiazolyl-o-phenylenediamine derivativeor salt takes place. Thus, for example, either monosubstituted ordisubstituted derivatives of the formulae ##STR6## in which R₁ is asdefined above, are obtained by treating a S-lower alkyl-isothiourea witha compound of the formula Cl-COOR₁.

In a typical reaction for the process described for the preparation ofcompounds of the formula I, hydrohalide salts of o-phenylenediaminecompounds of the formula II are reacted with one equivalent or with twoequivalents of a monoacyl- or S-diacyl-lower alkyl-isothiourea compound,in which acyl is a COOR₁ group, in aqueous solution in the presence ofan acid-binding agent, for example sodium acetate, at a temperature of30° to 200° C. and a pH value of 4-6. The reaction of an alkyl[bis-(alkylthioor arylthio)-methylene]-aminoformate with a compound ofthe formula II takes place with heating in an inert solvent, for exampletetrahydrofuran or dioxan.

In a further process variant, o-phenylenediamine derivatives of theformula II can be reacted with a monoor bis-(N-R₁ OOC)-cyanamide in anaqueous or alcoholic solution at a temperature of 30° to 200° C. and apH value of 4-9.

According to a second process, compounds of the formula I are obtainedby reacting a compound of the formula IV ##STR7## in which R₂ is asdefined above and R₃ and R₄ have the meanings defined above with theexception of hydrogen, with a compound of the formula V

    Hal--CO--X                                                 (V)

in which X is a halogen atom or the group -OR₁, and, if appropriate, ifa compound of the formula V is used in which X is halogen, replacing thehalogen atom in the resulting halogenocarbonylamino compound of theformula VI ##STR8## by the group -OR₁, and, if desired, carrying outadditional process steps.

The compounds of the formula V used for the reaction described arepreferably alkyl halogenoformates, especially lower alkylchloroformates. The reaction of the aminobenzimidazole derivative of theformula IV with a lower alkyl chloroformate takes place under theconditions customary for this reaction, i.e. in the presence of asuitable acid-binding agent, for example of an organic or inorganicbase, and of a suitable solvent. The reaction is preferably carried outwith heating at a temperature of from 50° C. to the reflux temperature.

However, the reaction described can also be carried out in two stepsusing a dihalide of carbonic acid, preferably using the dichloride(phosgene), and subsequently reacting the product with an alcohol togive the carbamate.

According to a third process, compounds of the general formula I areobtained by treating compounds of the general formula VII ##STR9## inwhich R₁, R₂, R₃ and R₄ are as defined above and n is the symbol 0 orthe integer 1, with an acid and, if desired, carrying out additionalprocess steps.

The acid used is preferably a mineral acid, for example sulfuric acid ora hydrogen halide acid, for example hydrochloric acid.

The conversion of a compound of the formula VII by treatment with amineral acid is preferably effected at elevated temperature, i.e. atabout 50° C. up to the reflux temperature, and, depending on the valueof the symbol n, the benzimidazole ring is formed by the detaching of asulfur atom or of sulfur monoxide.

Compounds of the general formula I are also obtained by a furtherprocess, by cyclising a o-aminothioallophanate of the formula VIII##STR10## in which R₁, R₂, R₃ and R₄ are as defined under formula I, inthe presence of an acid, preferably a mineral acid, and, if desired,carrying out additional process steps.

The cyclisation of an o-aminothioallophanate of the general formula VIIIto a benzimidazole derivative of the formula I is, if necessary, carriedout at elevated temperature, for example by heating under reflux in anaqueous mineral acid. The aqueous mineral acid used is, for example,dilute hydrochloric acid.

The compounds, according to the invention, of the formula I in which oneof the radicals R₃ and R₄ is hydrogen and the other has a meaningdefined for R₃ or R₄ other than hydrogen can be prepared by a furtherprocess, by detaching the amino protective group in compounds of theformula ##STR11## in which R₁ and R₂ are as defined above and one of thetwo substituents R₃ ' and R₄ ' is hydrogen or has the meaning definedfor R₃ or R₄ and the other is an amino protective group, and, ifdesired, carrying out additional process steps.

Protective groups R₃ ' and R₄ ' can be detached, for example, by meansof solvolysis or by reduction. Such groups are in particular acylradicals, especially of carbonic acid half-esters.

Amino protective groups R₃ ' and R₄ ' are, for example, 2-halogeno-loweralkoxycarbonyl groups, for example the 2,2,2-trichloroethoxycarbonylgroup or the 2-iodoethoxycarbonyl group, which can be detached byreduction by treatment with a metal or a corresponding metal salt, forexample by treatment with zinc in aqueous acetic acid or by treatmentwith a chromium-II salt, for example chromium-II chloride or chromium-IIacetate.

Further amino protective groups are suitable lower alkoxycarbonylgroups, such as tert.-butoxycarbonyl, which are detachable byacidolysis, for example by treatment with trifluoroacetic acid.

A further detachable amino protective group is an ethoxycarbonyl groupwhich in the β-position carries a silyl group substituted by threehydrocarbon radicals, such as a triphenylsilyl, dimethyl-butyl-silyl or,in particular, a trimethylsilyl group. A β-(tri-loweralkylsilyl)ethoxycarbonyl group of this type together with the aminogroup to be protected forms a corresponding β-tri-loweralkylsilyl-ethoxycarbonylamino group, which can be detached under mildconditions by the action of fluoride ions. Reagents which can be used asfluoride ion donors are, for example, fluorides of quaternary organicbases, such as tetraethylammonium fluoride.

a further group suitable as an amino protective group of this type is abenzyloxycarbonyl group, which can be substituted by a nitro group, forexample a p-nitrobenzyloxycarbonyl group, which can be detached by meansof hydrogen in the presence of palladium-on-charcoal as the catalyst or,if it is suitably substituted by nitro, by treatment with zinc andacetic acid.

A condition which must be observed is that only those amino protectivegroups which are selectively detachable whilst retaining the carbamateradical --NHCOOR₁ are suitable as amino protective groups R₃ ' and R₄ '.Furthermore, the keto group present should not be reduced.

The processes described can be carried out in the conventional manner atroom temperature, with cooling or warming, under normal pressure orelevated pressure and, if necessary, in the presence or absence of adiluent, catalyst or condensing agent. If necessary, the reactions canalso be carried out in the atmosphere of an inert gas, for examplenitrogen.

In resulting compounds, substituents can be introduced, modified ordetached, within the scope of the definition of the end products.

Depending on the process conditions and the starting materials, the endproducts are obtained in the free form or in the form of their salts,especially acid addition salts, which is also included in the invention.The acid addition salts of the novel compounds can be converted to thefree compound in a manner known per se, for example with basic agents,such as alkalis or ion exchangers. On the other hand, the resulting freebases can form salts with organic or inorganic acids. Acids used toprepare acid addition salts are in particular those which are suitablefor forming therapeutically usable salts. Examples of such acids are:hydrogen halide acids, sulfuric acids, phosphoric acids, nitric acid,perchloric acid and aliphatic, alicyclic, aromatic or heterocycliccarboxylic or sulfonic acids, such as formic acid, acetic acid,propionic acid, succinic acid, glycollic acid, lactic acid, malic acid,tartaric acid, citric acid, ascorbic acid, maleic acid, hydroxymaleicacid or pyruvic acid; phenylacetic acid, benzoic acid, p-aminobenzoicacid, anthranilic acid, p-hydroxybenzoic acid, salicylic acid orp-aminosalicylic acid, embonic acid, methanesulfonic acid,ethanesulfonic acid, hydroxyethanesulfonic acid or ethylenesulfonicacid; a halogenobenzenesulfonic acid, toluenesulfonic acid,naphthalenesulfonic acid or sulfanilic acid; and methionine, tryptophan,lysine or arginine.

These or other salts of the novel compounds, for example the picrates,can also be used to purify the resulting free bases, by converting thefree bases to salts, separating these off and liberating the bases againfrom the salts. Because of the close relationship between the novelcompounds in the free form and in the form of their salts, what isstated in this specification in respect of the free compounds alsoapplies by analogy to the corresponding salts.

The invention also relates to those embodiments of a process in which aprocess is discontinued at any stage or in which a compound obtainableas an intermediate at any stage is used as the starting material and themissing process steps are carried out, or a starting material is formedunder the reaction conditions or, if desired, is used in the form of asalt. The invention also includes novel intermediates resultingtherefrom.

The starting materials are known or, if they are novel, can be preparedby methods known per se.

Starting compounds of the formula II can be prepared by a sequence ofknown reaction steps using a 4-halogeno-3-nitro-acetophenone as thestarting material. Bromination of the active methylene group of theacetyl radical yields a compound of the formula X, which on reactionwith a thiourea derivative of the formula XI ##STR12## yields a compoundof the formula XII ##STR13## in which R₂, R₃ and R₄ are as defined underformula I and Hal is a halogen atom.

The reaction of a compound of the formula XII obtained in this way withaqueous or alcoholic ammonia, if necessary with the use of pressure anda catalyst, for example ethylene glycol, yields a nitroaniline of theformula XIII ##STR14## from which, in turn, the o-phenylenediaminederivative of the formula II, which is used as the starting material inthe first process, is obtained by reduction using a suitable reducingagent.

The reduction of the aromatic nitro compound of the formula XIII iseffected in a manner known per se, by hydrogenation in the presence of apalladium-on-charcoal catalyst in a suitable solvent. This reduction canalso be carried out by a chemical route, for example using metals, forexample zinc, in the presence of acids, preferably mineral acids, forexample hydrochloric acid, or alkanecarboxylic acids, for example aceticacid or trifluoroacetic acid. In specific cases glacial acetic acid canalso be used.

The bis-(alkylthio- or -arylthio)-methyleneaminoformates of the formula##STR15## which are used in the first process and in which R_(z) ¹ andR_(z) ² are an alkylthio or arylthio group are prepared by reacting abis-(alkylthio- or -arylthio)-methyleneamine with a halogenoformate,especially with a chloroformate. The monoacylated or bis-acylatedS-lower alkyl-isothioureas of the formula ##STR16## which are also usedin the first process and have already been mentioned briefly above areprepared by acylating S-lower alkyl-isothioureas with a chloroformate ina suitable solvent, for example water, and then treating the productwith a base, for example an aqueous alkali. The starting compounds usedfor this reaction are prepared and at the same time used in situ for thereaction.

The cyanamides of the formula NC--NH--COOR₁ mentioned in the process canbe obtained by reacting cyanamide with a suitable halogenoformate, forexample a chloroformate.

The starting compounds of the formula IV used in the second process canbe obtained by reacting a cyanogen halide, especially cyanogen bromide,with an o-phenylenediamine derivative of the formula II, as described inthe literature [J. Am. Chem. Soc. 69, 2459 (1947)].

The starting compounds of the formula VII which are used in the thirdprocess are obtained, in turn, by treating o-aminothioallophanates ofthe formula VIII with an oxidising agent, for example a halogen gas,especially bromine. Subsequent treatment with a per-acid yieldscompounds of the formula VII in which the symbol n is an integer 1.

The o-amino-thioallophanate of the formula VIII which is used in thefourth process is prepared by reacting an o-amino-phenylenediaminecompound of the formula II with an isothiocyanic acid derivative of theformula SCN--COOR₁. The reaction is preferably carried out in a solventwhich releases protons, for example an acid, if necessary with theapplication of heat.

The starting compounds of the formula IX used in the fifth process areprepared by reacting a modified o-phenylenediamine compound of theformula IIa ##STR17## in which one of the substituents R₃ ' and R₄ ' ishydrogen and the other is a detachable amino protective group, with acompound of the formula III ##STR18## in which R₁, R_(x) and R_(y) areas defined above. Starting compounds of the formula IIa are preparedanalogously to compounds of the formula II.

The invention also comprises therapeutic compositions of matter whichconsist of an anthelmintically active amount of the compounds of thegeneral formula I, or an acid addition salt, and a pharmacologicallyacceptable solid carrier or liquid diluents.

The pharmaceutical preparations according to the invention contain atleast one compound of the general formula I, or a salt thereof, as theactive ingredient, together with a conventional pharmaceutical carrier.The nature of the carriers largely depends on the field of application.The pharmaceutical compositions of matter according to the invention,which contain compounds of the formula I as active ingredients, can beadministered orally, parenterally or rectally.

Preparations suitable for the oral treatment of parasitic infections ofthe gastrointestinal tract, of the liver and of other organs are, inparticular, solid dosage unit forms, such as tablets, sugar-coatedtablets and capsules, which preferably contain between 10 and 90% of anactive ingredient of the general formula I, or of a salt, in order toenable daily doses of between 1.5 and 100 mg/kg to be administered towarm-blooded animals. To prepare tablets and sugar-coated tablet cores,the compounds of the general formula I are combined with solid,pulverulent carriers, such as lactose, sucrose, sorbitol, maize starch,potato starch or amylopectin, cellulose derivatives or gelatine,preferably with the addition of lubricants, such as magnesium stearateor calcium stearate, or polyethylene glycols of suitable molecularweight. Sugar-coated tablet cores are subsequently coated with, forexample, concentrated sugar solutions, which can additionally contain,for example, gum arabic, talc and/or titanium dioxide, or with a lacquerwhich is dissolved in readily volatile organic solvents or solventmixtures. Colorants can be added to these coatings, for example todistinguish different doses of active ingredient. Soft gelatine capsulesand other sealed capsules consist, for example, of a mixture of gelatineand glycerin and can contain, for example, mixtures of a compound of theformula I with polyethylene glycol. Dry-filled capsules contain, forexample, granules of an active ingredient with solid, pulverulentcarriers, for example lactose, sucrose, sorbitol or mannitol; starches,such as potato starch, maize starch or amylopectin, cellulosederivatives and gelatine as well as magnesium stearate or stearic acid.

Suitable dosage unit forms for rectal administration are, for example,suppositories, which consist of a combination of an active ingredientwith a suppository base based on natural or synthetic triglycerides (forexample cacao butter), polyethylene glycols or suitable higher fattyalcohols, and gelatine rectal capsules which contain a combination ofthe active ingredient with polyethylene glycols.

Ampoule solutions for parenteral, and in particular intramuscular orintravenous, administration contain a compound of the formula I or asalt thereof in a concentration of preferably 0.5 to 5% in the form ofan aqueous dispersion, prepared with the aid of conventionalsolubilising agents and/or emulsifiers and also, if necessary,stabilisers, or preferably contain an aqueous solution of apharmaceutically acceptable, water-soluble acid addition salt of acompound of the general formula I.

For liquids to be taken orally, such as syrups and elixirs, theconcentration of the active ingredient is so chosen that an individualdose can be measured out easily, for example as the contents of ateaspoon or of a measuring spoon, for example a 5 ml measuring spoon, oras a multiple of these volumes.

The following examples (a) to (e) will serve to illustrate thepreparation of some typical administration forms, but in no wayrepresent the only embodiments of such forms.

(a) 250.0 g of active ingredient are mixed with 550.0 g of lactose and292.0 g of potato starch and the mixture is moistened with an alcoholicsolution of 8 g of gelatine and granulated through a sieve. Afterdrying, 60.0 g of talc, 10.0 g of magnesium stearate and 20.0 g ofcolloidal silica are mixed in and the mixture is compressed to 10,000tablets each weighing 125 mg and containing 25 mg of active ingredient;if desired, the tablets can be provided with a breaking notch for fineradjustment of the dosage.

(b) Granules are prepared from 100.0 g of active ingredient, 379.0 g oflactose and an alcoholic solution of 6.0 g of gelatine and, afterdrying, these are mixed with 10.0 g of colloidal silica, 40.0 g of talc,60.0 g of potato starch and 5.0 g of magnesium stearate and the mixtureis compressed to 10,000 sugar-coated tablet cores. These are then coatedwith a concentrated syrup of 533.5 g of crystalline sucrose, 20.0 g ofShellack 75.0 g of gum arabic, 250.0 g of talc, 20.0 g of colloidalsilica and 1.5 g of a dye and dried. The resulting sugar-coated tabletseach weigh 150 mg and each contain 10 mg of active ingredient.

(c) 25.0 g of active ingredient and 1,975 g of finely ground suppositorybase (for example cacao butter) are mixed thoroughly and the mixture isthen melted. 1,000 2.0 g suppositories are cast from the melt, which iskept homogeneous by stirring. Each suppository contains 25 mg of activeingredient.

(d) To prepare a syrup containing 0.25% of active ingredient, 1.5 litersof glycerin, 42 g of methyl p-hydroxybenzoate, 18 g of n-propylp-hydroxybenzoate and, with gentle warming, 25.0 g of active ingredientare dissolved in 3 liters of distilled water, 4 liters of 70% sorbitolsolution, 1,000 g of crystalline sucrose, 350 g of glucose and an aromasubstance, for example 250 g of "Orange Peel Soluble Fluid" from EliLilly and Co., Indianapolis, or 5 g of natural lemon aroma and 5 g of"half and half" essence, both from Haarmann and Reimer, Holzminden,Germany, are added, the resulting solution is filtered and the filtrateis made up to 10 liters with distilled water.

(e) To prepare a drip solution containing 1.5% of active ingredient,150.0 g of active ingredient and 30 g of sodium cyclamate are dissolvedin a mixture of 4 liters of ethanol (96%) and 1 liter of propyleneglycol. A mixture of 3.5 liters of 70% sorbitol solution and 1 liter ofwater is prepared separately and added to the above solution of activeingredient. An aroma substance, for example 5 g of cough sweet aroma or30 g of Grapefruit Essence, both from Haarmann and Reimer, Holzminden,Germany, is then added and the whole is mixed well and filtered and thefiltrate is made up to 10 liters with distilled water.

The following examples illustrate the preparation of the novel compoundsof the general formula I without, however, restricting the scope of theinvention in any way. The temperatures are in degrees centigrade.

EXAMPLE 1

The "reagent" is prepared in situ as follows: A mixture of 4.2 g of5-methyl-isothiourea sulfate and 5 ml of water is cooled to 0°-2° withstirring and is treated at this temperature with 3.2 g of ethylchloroformate, which is added dropwise in the course of 10 minutes. Thereaction mixture is stirred for 15 minutes at the indicated temperatureand then treated with 5-6 ml of a 25% aqueous sodium hydroxide solutionuntil a pH value of 7.5-8 is obtained, the temperature being kept below5°. The mixture is stirred at this temperature for 15 minutes and thentreated at 0°-2° with 2 ml of glacial acetic acid, which is addeddropwise, the pH value being brought to 5-5.5.

A solution of 4 g of1,2-diamino-4-(4-methyl-2-methylamino-5-thiazolyl)-benzene in 150 ml ofmethanol is added all at once to the above reagent mixture. The reactionmixture is refluxed for 2 hours, with stirring, cooled to 0° andfiltered and the material on the filter is washed with 50% aqueousmethanol. The resulting solid material is purified by dissolving in2-normal hydrochloric acid and precipitating with ammonia and finally iswashed with water, yielding2-carboethoxyamino-5(6)-(4-methyl-2-methylamino-5-thiazoloyl)-benzimidazoleof the formula ##STR19## which melts at 280°-285° with decomposition.

The starting material for the above synthesis is prepared as follows: Amixture of 17 g of ethyl imidoacetate and 14 g of methyl isothiocyanateis warmed on a water bath for 2 hours and cooled and the adduct is usedas such in the next process step.

A solution of 30 g of the above adduct in 300 ml of isopropanol isrefluxed with 33 g of 4-chloro-3-nitrophenacyl bromide. After cooling,the solid material is filtered off and rendered basic with sodiumhydroxide, the mixture is filtered and the material on the filter iswashed with water and recrystallised from aqueous acetic acid, yielding4-chloro-3-nitro-1-(4-methyl-2-methylamino-5-thiazoloyl)-benzene, whichmelts at 220°-232°.

A mixture of 4 g of the above chlorine compound and 40 ml of analcoholic ammonia solution, which contains 0.2 ml of ethylene glycol, isheated in a bomb tube for 16 hours at 130°, cooled and filtered and theresidue is washed with water. The solid material is recrystallised fromaqueous acetic acid, yielding1-amino-2-nitro-4-(4-methyl-2-methylamino-5-thiazoloyl)-benzene, whichmelts at 260°-261° with decomposition.

A mixture of 40 g of stannous chloride dihydrate in 150 ml of aceticacid is saturated with dry hydrogen chloride gas and the above nitrocompound is then added in small portions, with stirring. The solution isstirred at 30° for a further 2 hours and the solvent is then evaporatedoff in vacuo. The residue is rendered basic with 50% aqueous potassiumhydroxide solution and the mixture is filtered. The residue is extractedwith hot methanol, the solvent is evaporated off and the residue isdigested with isopropanol. The product is recrystallised from methanol,yielding 1,2-diamino-4-(4-methyl-2-methylamino-5-thiazoloyl)-benzene inthe form of a hygroscopic solid material which melts at 115°-125°.

EXAMPLE 2

The reagent is prepared in situ analogously to Example 1, using 4.5 g ofS-methyl-isothiourea sulfate and 3.5 g of ethyl chloroformate as thestarting materials. A solution of 4.5 g of1,2-diamino-4-(4-methyl-2-ethylamino-5-thiazoloyl)-benzene in 100 ml ofmethanol is added to the resulting solution and the mixture is refluxedfor 2 hours. The reaction mixture is left to stand overnight at 30° andthe resulting solid material is filtered off, washed with hot methanoland purified by dissolving in 2-normal hydrochloric acid andprecipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-methyl-2-methylamino-5-thiazoloyl)-benzimidazole,which melts at 250°-255° (decomposition).

The starting material is prepared as follows: A mixture of 20 g of ethylimidoacetate and 20 g of ethyl isothiocyanate is warmed for 2 hours,with stirring. A mixture of 35 g of the resulting crude adduct and 56 gof 4-chloro-3-nitro-phenacyl bromide in 300 ml of isopropanol isrefluxed for 2 hours and worked up analogously to Example 1, yielding4-chloro-3-nitro-1-(4-methyl-2-ethylamino-5-thiazoloyl)-benzene, whichmelts at 195°.

A mixture of 4 g of the above chlorine compound and 0.4 g of ethyleneglycol in 40 ml of alcoholic ammonia solution is heated at 100° in abomb tube for 16 hours, cooled and filtered and the residue is washedwith water and recrystallised from aqueous acetic acid, yielding1-amino-2-nitro-4-(4-methyl-2-ethylamino-5-thiazoloyl)-benzene, whichmelts at 220°-225° (decomposition).

9 g of the above nitro compound are reduced with 45 g of stannouschloride in 150 ml of acetic acid and the reaction mixture is worked upanalogously to Example 1, yielding crude1,2-diamino-4-(4-methyl-2-ethylamino-5-thiazoloyl)-benzene, which meltsat 185°-225°.

EXAMPLE 3

The reagent is prepared in situ analogously to Example 1, using 8.5 g ofS-methyl-isothiourea sulfate and 6.5 g of ethyl chloroformate as thestarting materials. A solution of 9 g of1,2-diamino-4-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene in 100 mlof methanol is added to the solution and the mixture is refluxed for 4hours. After cooling, the precipitate is filtered off, washed with hotmethanol and purified by dissolving in 2-normal hydrochloric acid andprecipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzimidazolehemihydrate, which melts at 208°-212° (decomposition). The anhydrousproduct is prepared by washing with hot methanol and drying. Meltingpoint 229°-233°.

The base is converted to the hydrochloride by treating with ethanolichydrogen chloride and evaporating. A solution of 4.7 g of thishydrochloride in water is treated with a solution of 4.3 g of disodiumpamoate in 20 ml of water. The resulting precipitate is filtered off,washed with water and dried, yielding the corresponding pamoate, whichmelts at 240°-245° (decomposition).

The starting material is prepared as follows: 15 g of ethyl imidoacetateare reacted with 20 g of n-butyl isothiocyanate at 60° for 2 hours. Amixture of 10 g of the resulting adduct and 15 g of4-chloro-3-nitro-phenacyl bromide in 100 ml of isopropanol is refluxedfor 2 hours and evaporated, water is added to the residue and theresulting mixture is worked up analogously to Example 1, yielding4-chloro-3-nitro-1-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene, whichmelts at 125°-128°.

The same compound is also prepared as follows: 11.5 g of n-butylisothiocyanate are added to 11.4 g of N,N-diethyl-acetamidine, whereuponthe mixture becomes exothermic. The mixture is left to stand for 1 hourat 60° and the resulting adduct is used in the following experiment. Amixture of 22.9 g of the crude product and 27.9 g of4-chloro-3-nitro-phenacyl bromide in 200 ml of isopropanol is refluxedfor 2 hours. The solution is worked up as described above, yielding4-chloro-3-nitro-1-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene.

A solution of 30 g of the last-mentioned compound in 300 ml of alcoholicammonia is heated at 100° in a bomb tube for 20 hours, cooled andfiltered and the material on the filter is washed with water, affording1-amino-2-nitro-4-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene, whichmelts at 200°-205°.

50 g of the above nitro compound are added in portions in the course of20-30 minutes to a solution of 250 g of stannous chloride dihydrate in500 ml of concentrated hydrochloric acid, with stirring. The solution isstirred overnight at 30° and then evaporated in vacuo. The residue isdissolved in a minimal amount of water and the solution is cooled andrendered basic with potassium hydroxide. The resulting precipitate isfiltered off, washed with water and extracted with hot ethyl acetate.The extract is concentrated, treated with ether, cooled and filtered,yielding 1,2-diamino-4-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene,which melts at 127°-130°.

EXAMPLE 4

7 g of 1-amino-2-nitro-4-(4-methyl-2-isobutylamino-5-thiazoloyl)-benzeneare reduced with 40 g of stannous chloride in 150 ml of acetic acidanalogously to Example 1. Oily1,2-diamino-4-(4-methyl-2-isobutylamino-5-thiazoloyl)-benzene isobtained and this is used in the following step.

A solution of 3 g of the above diamine in 30 ml of methanol is added toa reagent solution which has been prepared beforehand (analogously toExample 1) from 2.8 g of S-methyl-isothiourea sulfate and 2.2 of ethylchloroformate. The solution is stirred and refluxed for 3 hours. Themethanol is distilled off and replaced by 50 ml of water and thereaction mixture is refluxed for 2 hours. The solution is cooled andfiltered and the residue is washed with water and recrystallised frommethanol, yielding2-carboethoxyamino-5(6)-(4-methyl-2-isobutylamino-5-thiazoloyl)-benzimidazolehemihydrate, which melts at 178°-180° (decomposition).

The starting material is prepared as follows: A mixture of 8.7 g ofethyl imidoacetate and 11.5 g of isobutyl isothiocyanate is kept at 60°for 4 hours. A mixture of 20 g of the resulting crude adduct and 26.8 gof 4-chloro-3-nitro-phenacyl bromide in 150 ml of isopropanol isrefluxed for 2 hours and the solvent is evaporated. The residue isrendered basic with sodium bicarbonate solution and extracted with ethylacetate. The extract is dried and evaporated. The residue isrecrystallised from a mixture of ethyl acetate and hexane, yielding4-chloro-3-nitro-1-(4-methyl-2-isobutylamino-5-thiazoloyl)-benzene,which melts at 138°-142°.

A solution of 9 g of the above chlorine compound in 150 ml of ethanolammonia is heated at 120° in a bomb tube for 12 hours and cooled and thesolvent is evaporated off. Water is added to the residue, the mixture isfiltered and the material on the filter is dried, yielding1-amino-2-nitro-4-(4-methyl-2-isobutylamino-5-thiazoloyl)-benzene, whichmelts at 210°-215°.

EXAMPLE 5

5.5 g of1-amino-2-nitro-4-(4-methyl-2-n-pentylamino-5-thiazolyl)-benzene arereduced with 25 g of stannous chloride in 100 ml of acetic acid,analogously to Example 1. The resulting gum-like diamine is employed inthe subsequent cyclisation.

A solution of 3.8 g of the above diamine in 50 ml of methanol is addedto a reagent solution which has been prepared beforehand (analogously toExample 1) from 3.4 g of S-methyl-isothiourea sulfate and 2.7 g of ethylchloroformate. The solution is stirred and refluxed for 3 hours. Themethanol is distilled off and replaced by 50 ml of water and thereaction mixture is refluxed for 2 hours. The solution is cooled andfiltered and the residue is washed with water and recrystallised fromaqueous acetic acid, yielding2-carboethoxyamino-5(6)-(4-methyl-2-n-pentylamino-5-thiazoloyl)-benzimidazole,which melts at 220°-224°.

The starting material is prepared as follows: A mixture of 8.7 g ofethyl imidoacetate and 12.9 g of n-pentyl isothiocyanate is kept at 60°for 4 hours. A mixture of 21 g of the resulting crude adduct with 27 gof 4-chloro-3-nitro-phenacyl bromide in 150 ml of isopropanol isrefluxed for 2 hours and the solvent is evaporated. The product isrendered basic with sodium bicarbonate, extracted with ethyl acetate andrecrystallised from a mixture of ethyl acetate and hexane, yielding4-chloro-3-nitro-1-(4-methyl-2-n-pentylamino-5-thiazoloyl)-benzene,which melts at 99°-104°.

A solution of 9 g of the above chlorine compound in 150 ml of ethanolicammonia is heated at 80° in a bomb tube for 24 hours and cooled and thesolvent is evaporated off. Water is added to the residue, the mixture isfiltered and the material on the filter is dried and recrystallised froman ethyl acetate/hexane mixture, yielding1-amino-2-nitro-4-(4-methyl-2-n-pentylamino-5-thiazoloyl)-benzene, whichmelts at 165°-169°.

EXAMPLE 6

The reagent is prepared analogously to Example 1, using 1.4 g ofS-methyl-isothiourea sulfate and 1.2 g of ethyl chloroformate as thestarting materials. A solution of 1.8 g of1,2-diamino-4-(4methyl-2-allylamino-5-thiazoloyl)-benzenedihydrochloride in 20 ml of water and then a solution of 1.4 g of sodiumacetate trihydrate in 4 ml of water are added to the resulting solution.The reaction mixture is refluxed for 2 hours, cooled and filtered. Theresulting precipitate is washed with water and then with hot methanol.The product is purified by dissolving in 2-normal hydrochloric acid andprecipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-methyl-2-allylamino-5-thiazoloyl)-benzimidazole,which melts at 210°-219° (decomposition).

The starting material is prepared as follows: A mixture of 8.7 g ofethyl imidoacetate and 10 g of allyl isothiocyanate is kept at 60° for 4hours. 10 g of the resulting crude adduct and 15 g of4-chloro-3-nitrophenacyl bromide in 80 ml of isopropanol are refluxedfor 2 hours and the solvent is evaporated off. The product is renderedbasic and extracted with ethyl acetate. The solvent is evaporated offand the residue is recrystallised from a mixture of ethyl acetate andhexane, yielding4-chloro-3-nitro-1-(4-methyl-2-allylamino-5-thiazoloyl)-benzene, whichmelts at 154°-156°.

A solution of 4.5 g of the above chlorine compound in 200 ml ofethanolic ammonia is heated at 120° in a bomb tube for 12 hours, cooledand filtered. The residue is treated with water, dried andrecrystallised from aqueous acetic acid, yielding1-amino-2-nitro-4-(4-methyl-2-allylamino-5-thiazoloyl)-benzene, whichmelts at 250°-252°.

The last-mentioned nitro compound is reduced analogously to Example 1with 8 g of stannous chloride dihydrate in 50 ml of acetic acid andyields 1,2-diamino-4-(4-methyl-2-allylamino-5-thiazoloyl)-benzene, whichis isolated in the form of the dihydrochloride. The product shrinks at250° and does not melt up to 350°.

EXAMPLE 7

2.8 g of 1-amino-2-nitro-4-(4-methyl-2-anilino-5-thiazoloyl)-benzene arereduced analogously to Example 1 with 15 g of stannous chloride in 60 mlof acetic acid and the resulting oily diamine is used in the subsequentcyclisation.

A solution of 2.8 g of the above diamine in 50 ml of methanol is addedto a reagent solution which has been prepared beforehand (analogously toExample 1) from 2.8 g of S-methyl-isothiourea sulfate and 2.2 g of ethylchloroformate. The solution is stirred and refluxed for 3 hours. Thereaction mixture is cooled and filtered and the residue is washed withwater and recrystallised from aqueous acetic acid, yielding2-carboethoxyamino-5(6)-(4-methyl-2-anilino-5-thiazoloyl)-benzimidazole,which melts at 250°-255° (decomposition).

The starting material is prepared as follows: A mixture of 8.7 g ofethyl imidoacetate and 13.5 g of phenyl isothiocyanate is kept at 60°for one hour and triturated with hexane and the residue is filtered off.The adduct, which melts at 96°-98°, is obtained. It is recrystallisedfrom a mixture of ethyl acetate/hexane.

10 g of the adduct and 13 g of 4-chloro-3-nitrophenacyl bromide in 100ml of isopropanol are refluxed for 2 hours. The solvent is removed invacuo and the residue is rendered basic with sodium bicarbonate solutionand extracted with ethyl acetate. The extract is dried, concentrated andtreated with hexane, yielding4-chloro-3-nitro-1-(4-methyl-2-anilino-5-thiazoloyl)-benzene, whichmelts at 162°-165°.

A solution of 3.5 g of the above chlorine compound in 50 ml of ethanolicammonia is heated at 80° in a bomb tube for 24 hours. The solution iscooled, concentrated to a small volume and filtered. The residue iswashed with water and recrystallised from aqueous acetic acid, yielding1-amino-2-nitro-4-(4-methyl-2-anilino-5-thiazoloyl)-benzene, which meltsat 235°-239°.

EXAMPLE 8

The reagent is prepared in situ analogously to Example 1 but methylchloroformate is used in place of ethyl chloroformate: 8.4 g ofS-methyl-isothiourea sulfate and 5.7 g of methyl chloroformate.

A solution of 9.1 g of1,2-diamino-4-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzene (which isprepared analogously to Example 3) in 200 ml of methanol is added to theresulting solution and the mixture is refluxed for 4 hours. Aftercooling, the precipitate is filtered off, washed with hot methanol andpurified by dissolving in 2 normal hydrochloric acid and precipitatingwith ammonia, yielding2-carbomethoxyamino-5(6)-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzimidazole,which melts at 241°-243° (decomposition).

EXAMPLE 9

The reagent is prepared in situ analogously to example 1, using 1.7 g ofS-methyl-isothiourea sulfate and 1.4 g of ethyl chloroformate. First asolution of 2 g of1,2-diamino-4-(4-ethyl-2-methylamino-5-thiazoloyl)-benzenedihydrochloride in 20 ml of water and then a solution of 1.7 g of sodiumacetate trihydrate in 5 ml of water are added to the resulting solution.The reaction mixture is stirred and boiled under reflux for 2 hours,cooled and filtered. The residue is washed with water and then with hotmethanol and purified by dissolving in 2 normal hydrochloric acid andprecipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-ethyl-2-methylamino-5-thiazoloyl)-benzimidazolehemihydrate, which melts at 204°-208° (decomposition).

The starting material is prepared as follows: A mixture of 12 g of ethylimidopropionate and 8.4 g of methyl isothiocyanate is kept at 70° for 2hours. 20.4 g of the resulting crude adduct and 30 g of4-chloro-3-nitro-phenacyl bromide in 150 ml of isopropanol are refluxedfor 2 hours and the solvent is evaporated off. The product is renderedbasic and extracted with methylene chloride. The extract is dried andevaporated and the residue is recrystallised from a mixture of ethylacetate and hexane, yielding4-chloro-3-nitro-1-(4-ethyl-2-methylamino-5-thiazoloyl)-benzene, whichmelts at 186°-190°.

A solution of 4 g of the above chlorine compound in 100 ml of ethanolicammonia is heated at 120° in a steel tube for 8 hours and cooled and thesolvent is evaporated. The residue is digested with water, the mixtureis filtered and the material on the filter is recrystallised fromaqueous isopropanol, yielding1-amino-2-nitro-4-(4-ethyl-2-methylamino-5-thiazoloyl)-benzene, whichmelts at 210°-215°.

5 g of the above nitro compound are reduced analogously to Example 1with 25 g of stannous chloride in 100 ml of acetic acid. The product isconverted to its dihydrochloride using ethanolic hydrogen chloride.After triturating with hot isopropanol,1,2-diamino-4-(4-ethyl-2-methylamino-5-thiazoloyl)-benzenedihydrochloride is obtained, which melts at 231°-236° (decomposition).

EXAMPLE 10

5.5 g of 1-amino-2-nitro-4-(4-ethyl-2-ethylamino-5-thiazoloyl)-benzeneare reduced analogously to Example 1 with 30 g of stannous chloride in100 ml of acetic acid. The product is converted to its dihydrochlorideusing hydrogen chloride in isopropanol and this product is filtered offand used immediately for the subsequent cyclisation.

A solution of 2 g of the above dihydrochloride of1,2-diamino-4-(4-ethyl-2-ethylamino-5-thiazoloyl)-benzene in 20 ml ofwater is added to a reagent solution which has been prepared beforehand(analogously to Example 1) from 1.7 g of S-methyl-isothiourea sulfateand 1.4 g of ethyl chloroformate, and 1.7 g of sodium acetate trihydratein 4 ml of water are then added to the mixture. The mixture is stirredand boiled under reflux for 2 hours, cooled and filtered. The residue iswashed with water and hot methanol and purified by dissolving in B2-normal hydrochloric acid and precipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-ethyl-2-ethylamino-5-thiazoloyl)-benzimidazole,which melts at 217°-220°.

The starting material is prepared as follows: A mixture of 10 g of ethylimidopropionate and 10 g of ethyl isothiocyanate is heated at 70° for 2hours and the crude adduct is used in the subsequent reaction. A mixtureof 13.5 g of the said product and 21 g of 4-chloro-3-nitro-phenacylbromide in 150 ml of isopropanol is refluxed for 2 hours, cooled andfiltered. The filtrate is evaporated in vacuo and the residue isrendered basic with sodium bicarbonate solution and extracted with ethylacetate. The extract is dried and evaporated and the residue isrecrystallised from a mixture of ethyl acetate and hexane, yielding4-chloro-3-nitro-1-(4-ethyl-2-ethylamino-5-thiazoloyl)-benzene, whichmelts at 149°-152°.

A solution of 8 g of the above chlorine compound in 150 ml of ethanolicammonia is heated at 120° in a steel tube for 14 hours. The reactionmixture is cooled and the solvent is evaporated off. The residue isdigested with water, the mixture is filtered and the material on thefilter is dried and recrystallised from a mixture of ethyl acetate andhexane, yielding1-amino-2-nitro-4-(4-ethyl-2-ethylamino-5-thiazoloyl)-benzene, whichmelts at 210°-212°.

EXAMPLE 11

The reagent is prepared in situ analogously to Example 1, using 2.8 g ofS-methylisothiourea sulfate and 2.2 g of ethyl chloroformate as thestarting materials. A solution of 2.8 g of1,2-diamino-4-(4-methyl-2-dimethylamino-5-thiazoloyl)-benzene in 80 mlof methanol is added to the resulting solution and the mixture isrefluxed for 2 hours. The solution is cooled and evaporated, the residueis digested with water and the mixture is filtered. The residue iswashed with hot methanol and purified by dissolving in 2 normalhydrochloric acid and precipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-methyl-2-dimethylamino-5-thiazoloyl)-benzimidazolemonohydrate, which melts at 270°-275° (decomposition).

The starting material is prepared as follows: A mixture of 3.7 g ofN-acetyl-N',N'-dimethyl-thiourea and 7 g of 4-chloro-3-nitro-phenacylbromide in 100 ml of isopropanol is refluxed for 2 hours, cooled andfiltered. The residue is rendered basic and extracted with methylenechloride. The extract is dried and evaporated and the residue isrecrystallised from a mixture of ethyl acetate and hexane, yielding4-chloro-3-nitro-1-(4-methyl-2-dimethylamino-5-thiazoloyl)-benzene,which melts at 165°-169°.

A mixture of 3.5 g of the above chlorine compound and 0.5 ml of ethyleneglycol in 40 ml of alcoholic ammonia is heated at 130° in a bomb tubefor 16 hours. The product is filtered off, washed with water andrecrystallised from a mixture of ethyl acetate and hexane, yielding1-amino-2-nitro-4-(4-methyl-2-dimethylamino-5-thiazoloyl)-benzene, whichmelts at 225°-228°.

7 g of the above nitro compound are reduced analogously to Example 1with 40 g of stannous chloride in 150 ml of acetic acid. The product isextracted with methylene chloride and the extract is dried andevaporated. The residue is recrystallised from isopropanol, yielding1,2-diamino-4-(4-methyl-2-dimethylamino-5-thiazoloyl)-benzene, whichmelts at 174°-178°.

EXAMPLE 12

The reagent is prepared in situ analogously to Example 1, using 2.8 g ofS-methyl-isothiourea sulfate and 2.2 g of ethyl chloroformate as thestarting materials. A solution of 3.8 g of1,2-diamino-4-(4-methyl-2-pyrrolidinyl-5-thiazoloyl)-benzenedihydrochloride in 20 ml of water and then a solution of 2.8 g of sodiumacetate trihydrate in 8 ml of water are added to the resulting solution.The reaction mixture is stirred and refluxed for 2 hours, cooled andfiltered. The residue is washed, first with water and then with hotmethanol, and purified by dissolving in 2 normal hydrochloric acid andprecipitating with ammonia, yielding2-carboethoxyamino-5(6)-(4-methyl-2-pyrrolidinyl-5-thiazoloyl)-benzimidazolehemihydrate, which melts at 185°-195° (decomposition).

The starting material is prepared as follows: A mixture of 10 g ofmethyl N-acetyl-dithiocarbamate and 5 g of pyrrolidine in 100 ml ofethanol is kept at 30° for 16 hours, the solvent is evaporated off invacuo and the residue is recrystallised from a mixture of ethyl acetateand hexane, yielding pyrrolidinothiocarbonylacetamide, which melts at110°-120°.

A mixture of the last-mentioned thiourea derivative and 16.8 g of4-chloro-3-nitro-phenacyl bromide in 200 ml of isopropanol is refluxedfor 3 hours and evaporated. The residue is digested with water, renderedbasic with sodium bicarbonate solution and extracted with ethyl acetate.The extract is dried, concentrated, cooled and filtered, yielding4-chloro-3-nitro-1-(4-methyl-2-pyrrolidinyl-5-thiazoloyl)-benzene, whichmelts at 168°-171°.

A solution of 4 g of the above chlorine compound in 100 ml of ethanolicammonia is heated at 120° in a steel tube for 8 hours, cooled andfiltered. The residue is washed with water and recrystallised fromaqueous acetic acid, yielding1-amino-2-nitro-4-(4-methyl-2-pyrrolidinyl-5-thiazoloyl)-benzene, whichmelts at 245°-248° (decomposition).

6 g of the above nitro compound are reduced analogously to Example 1with 30 g of stannous chloride in 100 ml of acetic acid. The product isconverted to its hydrochloride using hydrogen chloride in ethanol, thisproduct is digested with hot isopropanol and the mixture is filtered,yielding 1,2-diamino-4-(4-methyl-2-pyrrolidinyl-5-thiazoloyl)-benzenedihydrochloride, which melts at 210°-220° (decomposition).

EXAMPLE 13

4 g of 1-amino-2-nitro-4-(2-n-butylamino-5-thiazoloyl)-benzene arereduced analogously to Example 1 with 20 g of stannous chloride in 100ml of acetic acid. The resulting crude diamine is used in the subsequentcyclisation.

A solution of 4 g of the above diamine in 50 ml of methanol is added toa reagent solution which has been prepared beforehand (analogously toExample 1) from 4.2 g of S-methyl-isothiourea sulfate and 3.2 g of ethylchloroformate. The solution is stirred and refluxed for 3 hours. Themethanol is distilled off and replaced by 50 ml of water and thereaction mixture is refluxed for 2 hours. The solution is cooled andfiltered and the precipitate is washed with water. The product ispurified by dissolving in 2 normal hydrochloric acid and precipitatingwith ammonia, yielding 2-carboethoxyamino5(6)-(2-n-butylamino-5-thiazoloyl)-benzimidazole, which melts at295°-300° (decomposition).

The starting material is prepared as follows: A mixture of 5 g ofN-butyl-thiourea and 15 ml of dimethylformamide dimethyl acetal isrefluxed for 6 hours and the excess DMF acetal is evaporated off invacuo. The residue is used in the subsequent condensation reaction.

7 g of the resulting imidoylthiourea and 11 g of4-chloro-3-nitro-phenacyl bromide in 100 ml of isopropanol are refluxedfor 1 hour. The solvent is evaporated off, the residue is digested withwater and ethyl acetate and the mixture is filtered. The solid materialis recrystallised from ethyl acetate, yielding4-chloro-3-nitro-1-(2-n-butylamino-5-thiazoloyl)-benzene, which melts at192°-194°.

8 g of the above chlorine compound are taken and heated with 150 ml ofethanolic ammonia at 80° in a steel tube for 24 hours. The reactionmixture is cooled and filtered and the residue is washed with water,dried and recrystallised from ethyl acetate, yielding1-amino-2-nitro-4-(2-n-butylamino-5-thiazoloyl)-benzene, which melts at198°-203°.

EXAMPLE 14

5 g of 1-amino-2-nitro-4-(2-cyclohexylamino-5-thiazoloyl)-benzene arereduced analogously to Example 1 with 25 g of stannous chloride in 125ml of acetic acid. The resulting crude diamine is used in the subsequentcyclisation.

A solution of 4.5 g of the above diamine in 50 ml of methanol is addedto a reagent solution which has been prepared beforehand (analogously toExample 1) from 4.2 g of S-methyl-isothiourea sulfate and 3.2 g of ethylchloroformate. The solution is stirred and refluxed for 2 hours. Themethanol is then distilled off and replaced by 50 ml of water and themixture is refluxed for a further 2 hours. The solution is cooled andfiltered and the residue is washed with water and purified by dissolvingin 2 normal hydrochloric acid and precipitating with aqueous ammonia.The precipitate is filtered off, washed with water, dried, digested withhot ethyl acetate and filtered off again, yielding2-carboethoxyamino-5(6)-(2-cyclohexylamino-5-thiazoloyl)-benzimidazole,which melts at 216°-219° (decomposition).

The starting material is prepared as follows: A mixture of 5 g ofN-cyclohexylthiourea and 10 ml of dimethylformamide dimethyl acetal isrefluxed for 6 hours and the excess DMF acetal is removed in vacuo. Theresidue is digested with hexane and the solid material is recrystallisedfrom a mixture of ethyl acetate and hexane, yieldingN,N-dimethyl-N'-cyclohexyl-thiocarbamylformamidine, which melts at116°-120°.

5 g of the last-mentioned compound and 7 g of 4-chloro-3-nitro-phenacylbromide in 100 ml of isopropanol are refluxed for 2 hours. The solventis evaporated off, the residue is digested with water and ether, themixture is filtered and the material on the filter is recrystallisedfrom ethyl acetate, yielding4-chloro-3-nitro-1-(2-cyclohexylamino-5-thiazoloyl)-benzene, which meltsat 194°-198°.

A solution of 6 g of the last-mentioned compound in 150 ml of ethanolicammonia is heated at 80° in a steel tube for 24 hours, cooled andfiltered. The residue is washed with water and recrystallised fromaqueous acetic acid, yielding1-amino-2-nitro-4-(2-cyclohexylamino-5-thiazoloyl)-benzene, which meltsat 245°-250°.

What is claimed is: 1.2-Carbomethoxyamino-5(6)-(4-methyl-2-n-butylamino-5-thiazoloyl)-benzimidazoleand a therapeutically acceptable salt thereof.
 2. A therapeuticcomposition for the treatment of parasitic infections by helminthscomprising an effective amount of an anthelmintic active compound ofclaim 1, together with a parmaceutically acceptable excipient.
 3. Amethod for the treatment of parasitic infections by helminths whichcomprises administering to a living body suffering from parasiticinfections an effective amount of a compound of claim 1.